nsv3919429
- Organism: Homo sapiens
- Study:nstd102 (Clinical Structural Variants)
- Variant Type:copy number variation
- Method Type:Multiple
- Submitted on:GRCh37, GRCh38, NCBI36
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:13,642,237
- Description:GRCh38/hg38 22q11.21-12.3(chr22:18178957-31821193)x3 AND See cases
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 46147 SVs from 147 studies. See in: genome view
Overlapping variant regions from other studies: 47276 SVs from 148 studies. See in: genome view
Overlapping variant regions from other studies: 14681 SVs from 41 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Assembly | Assembly Unit | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nsv3919429 | Submitted genomic | GRCh38 (hg38) | Primary Assembly | NC_000022.11 | Chr22 | 18,178,957 | 31,821,193 |
| nsv3919429 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000022.10 | Chr22 | 18,661,724 | 32,217,179 |
| nsv3919429 | Submitted genomic | NCBI36 (hg18) | Primary Assembly | NC_000022.9 | Chr22 | 17,041,724 | 30,547,179 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15132566 | copy number gain | Multiple | Multiple | See cases | Pathogenic | ClinVar | RCV000050768.6, VCV000057132.1 | 3 |
Variant Call Placement Information
| Variant Call ID | Placement Type | HGVS | Assembly | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|
| nssv15132566 | Submitted genomic | NC_000022.11:g.(?_ 18178957)_(3182119 3_?)dup | GRCh38 (hg38) | NC_000022.11 | Chr22 | 18,178,957 | 31,821,193 |
| nssv15132566 | Submitted genomic | NC_000022.10:g.(?_ 18661724)_(3221717 9_?)dup | GRCh37 (hg19) | NC_000022.10 | Chr22 | 18,661,724 | 32,217,179 |
| nssv15132566 | Submitted genomic | NC_000022.9:g.(?_1 7041724)_(30547179 _?)dup | NCBI36 (hg18) | NC_000022.9 | Chr22 | 17,041,724 | 30,547,179 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Allele Origin | Subject Phenotype | Clinical Interpretation | Source of Interpretation | ClinVar ID | Copy number |
|---|---|---|---|---|---|---|---|---|
| nssv15132566 | GRCh37: NC_000022.10:g.(?_18661724)_(32217179_?)dup, GRCh38: NC_000022.11:g.(?_18178957)_(31821193_?)dup, NCBI36: NC_000022.9:g.(?_17041724)_(30547179_?)dup | copy number gain | not provided | See cases | Pathogenic | ClinVar | RCV000050768.6, VCV000057132.1 | 3 |